Concept information
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Coagulation Protein Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Término preferido
von Willebrand Diseases
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Tipo
-
mesh:Descriptor
Definición
- Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Concepto genérico
Conceptos específicos
Etiquetas alternativas
- Angiohemophilia
- Hemophilia, Vascular
- Vascular Pseudohemophilia
- von Willebrand Disease
- Von Willebrand Disorder
- von Willebrand's Disease
- von Willebrand's Diseases
- Von Willebrand's Factor Deficiency
En otras lenguas
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francés
-
Angiohémophilie
-
Angiohémophilies
-
Hémophilie vasculaire
-
Maladie de von Willebrand
-
Maladie de Willebrand
-
Maladie Von Willebrand
URI
http://data.loterre.fr/ark:/67375/JVR-SHW72XVB-3
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